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Growth hormone deficiency testing and treatment following mild traumatic brain injury
Pituitary dysfunction, specifically growth hormone (GH) deficiency, can occur following traumatic brain injury. Our objective was to characterize the prevalence of GH deficiency (GHD) testing and response to recombinant human GH (rhGH) treatment in adults with persistent symptoms following mild trau...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058058/ https://www.ncbi.nlm.nih.gov/pubmed/33879807 http://dx.doi.org/10.1038/s41598-021-87385-7 |
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author | Mercier, Leah J. Kruger, Natalia Le, Quynk B. Fung, Tak S. Kline, Gregory A. Debert, Chantel T. |
author_facet | Mercier, Leah J. Kruger, Natalia Le, Quynk B. Fung, Tak S. Kline, Gregory A. Debert, Chantel T. |
author_sort | Mercier, Leah J. |
collection | PubMed |
description | Pituitary dysfunction, specifically growth hormone (GH) deficiency, can occur following traumatic brain injury. Our objective was to characterize the prevalence of GH deficiency (GHD) testing and response to recombinant human GH (rhGH) treatment in adults with persistent symptoms following mild traumatic brain injury (mTBI) referred for assessment of pituitary dysfunction. A retrospective chart review was conducted of patients seen at an outpatient brain injury clinic with a diagnosis of mTBI and persistent post-concussive symptoms who were referred to endocrinology. Clinical assessments of symptoms were collected. Investigations and results of GHD were collected, including initiation of rhGH treatment and treatment response. Of the 253 patients seen in both brain injury and endocrinology clinics, 97 with mTBI were referred for investigation of pituitary dysfunction and 73 (75%) had dynamic testing for assessment of GHD. Of the 26 individuals diagnosed with GHD, 23 (88%) started rhGH. GH therapy was inconsistently offered based on interpretation of GH dynamic testing results. Of those who started rhGH, 18 (78%) had a useful treatment response. This study suggests that clinical management of these patients is varied, highlighting a need for clear guidelines for the diagnosis and management of GHD following mTBI. |
format | Online Article Text |
id | pubmed-8058058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80580582021-04-22 Growth hormone deficiency testing and treatment following mild traumatic brain injury Mercier, Leah J. Kruger, Natalia Le, Quynk B. Fung, Tak S. Kline, Gregory A. Debert, Chantel T. Sci Rep Article Pituitary dysfunction, specifically growth hormone (GH) deficiency, can occur following traumatic brain injury. Our objective was to characterize the prevalence of GH deficiency (GHD) testing and response to recombinant human GH (rhGH) treatment in adults with persistent symptoms following mild traumatic brain injury (mTBI) referred for assessment of pituitary dysfunction. A retrospective chart review was conducted of patients seen at an outpatient brain injury clinic with a diagnosis of mTBI and persistent post-concussive symptoms who were referred to endocrinology. Clinical assessments of symptoms were collected. Investigations and results of GHD were collected, including initiation of rhGH treatment and treatment response. Of the 253 patients seen in both brain injury and endocrinology clinics, 97 with mTBI were referred for investigation of pituitary dysfunction and 73 (75%) had dynamic testing for assessment of GHD. Of the 26 individuals diagnosed with GHD, 23 (88%) started rhGH. GH therapy was inconsistently offered based on interpretation of GH dynamic testing results. Of those who started rhGH, 18 (78%) had a useful treatment response. This study suggests that clinical management of these patients is varied, highlighting a need for clear guidelines for the diagnosis and management of GHD following mTBI. Nature Publishing Group UK 2021-04-20 /pmc/articles/PMC8058058/ /pubmed/33879807 http://dx.doi.org/10.1038/s41598-021-87385-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mercier, Leah J. Kruger, Natalia Le, Quynk B. Fung, Tak S. Kline, Gregory A. Debert, Chantel T. Growth hormone deficiency testing and treatment following mild traumatic brain injury |
title | Growth hormone deficiency testing and treatment following mild traumatic brain injury |
title_full | Growth hormone deficiency testing and treatment following mild traumatic brain injury |
title_fullStr | Growth hormone deficiency testing and treatment following mild traumatic brain injury |
title_full_unstemmed | Growth hormone deficiency testing and treatment following mild traumatic brain injury |
title_short | Growth hormone deficiency testing and treatment following mild traumatic brain injury |
title_sort | growth hormone deficiency testing and treatment following mild traumatic brain injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058058/ https://www.ncbi.nlm.nih.gov/pubmed/33879807 http://dx.doi.org/10.1038/s41598-021-87385-7 |
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